Team:The University of Alberta/26 October 2008

From 2008.igem.org

(Difference between revisions)
(David)
(Jason)
 
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I performed a mini-prep of pUC57-ER, subsequently digesting it with XbaI and PstI, gel purifying the fragment and using it one of the following ligations.
I performed a mini-prep of pUC57-ER, subsequently digesting it with XbaI and PstI, gel purifying the fragment and using it one of the following ligations.
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I set up ligations for of pSB103+ER, pSB103+laqIQ-ERE-TetR-pTET-RFP, pSB103+pTET-BisdA-pTET-BisdB, pUC57-laqIQ-ERE-TetR-pTET-RFP+pTET-BisdA-pTET-BisdB and left them overnight at 16 degrees C.
+
I set up ligations for of pSB1A3+ER, pSB1A3+laqIQ-ERE-TetR-pTET-RFP, pSB1A3+pTET-BisdA-pTET-BisdB, pUC57-laqIQ-ERE-TetR-pTET-RFP+pTET-BisdA-pTET-BisdB and left them overnight at 16 degrees C.
i was awesome today.
i was awesome today.

Latest revision as of 03:23, 29 October 2008

Jason

I performed a mini-prep of pUC57-ER, subsequently digesting it with XbaI and PstI, gel purifying the fragment and using it one of the following ligations.

I set up ligations for of pSB1A3+ER, pSB1A3+laqIQ-ERE-TetR-pTET-RFP, pSB1A3+pTET-BisdA-pTET-BisdB, pUC57-laqIQ-ERE-TetR-pTET-RFP+pTET-BisdA-pTET-BisdB and left them overnight at 16 degrees C.

i was awesome today.

David

yesterday's transformations didn't work. not at all. no colonies. what is up with that?